Genome-wide identification and expression analysis reveals spinach brassinosteroid-signaling kinase (BSK) gene family functions in temperature stress response

Background Brassinosteroid (BR)- signaling kinase (BSK) is a critical family of receptor-like cytoplasmic kinase for BR signal transduction, which plays important roles in plant development, immunity, and abiotic stress responses. Spinach (Spinacia oleracea) is cold- tolerant but heat- sensitive green leafy vegetable. A study on BSK family members and BSKs- mediated metabolic processes in spinach has not been performed. Results We identified and cloned seven SoBSKs in spinach. Phylogenetic and collinearity analyses suggested that SoBSKs had close relationship with dicotyledonous sugar beet (Beta vulgaris) rather than monocotyledons. The analyses of gene structure and conserved protein domain/ motif indicated that most SoBSKs were relative conserved, while SoBSK6 could be a truncated member. The prediction of post-translation modification (PTM) sites in SoBSKs implied their possible roles in signal transduction, redox regulation, and protein turnover of SoBSKs, especially the N-terminal myristoylation site was critical for BSK localization to cell periphery. Cis-acting elements for their responses to light, drought, temperature (heat and cold), and hormone distributed widely in the promoters of SoBSKs, implying the pivotal roles of SoBSKs in response to diverse abiotic stresses and phytohormone stimuli. Most SoBSKs were highly expressed in leaves, except for SoBSK7 in roots. Many SoBSKs were differentially regulated in spinach heat- sensitive variety Sp73 and heat- tolerant variety Sp75 under the treatments of heat, cold, as well as exogenous brassinolide (BL) and abscisic acid (ABA). The bsk134678 mutant Arabidopsis seedlings exhibited more heat tolerance than wild- type and SoBSK1- overexpressed seedlings. Conclusions A comprehensive genome- wide analysis of the BSK gene family in spinach presented a global identification and functional prediction of SoBSKs. Seven SoBSKs had relatively- conserved gene structure and protein function domains. Except for SoBSK6, all the other SoBSKs had similar motifs and conserved PTM sites. Most SoBSKs participated in the responses to heat, cold, BR, and ABA. These findings paved the way for further functional analysis on BSK- mediated regulatory mechanisms in spinach development and stress response. Supplementary Information The online version contains supplementary material available at 10.1186/s12864-022-08684-5.


Introduction
Spinach (Spinacia oleracea) is an important and nutritious green leafy vegetable, which belongs to the Amaranthaceae family [1]. Generally, spinach is cold-tolerant but heat-sensitive vegetable species, which limits its distribution and production in tropics [2]. Under 37 °C/ 32 °C (day/night) treatment for 24 h, we found that the relative water content in leaves from heat-sensitive variety Sp73 was decreased to 66.1%, which was obviously lower than that in heat-tolerant variety Sp75 (75.7%) [3,4]. The genomics analysis on spinach presented a high-quality chromosome-scale reference genome, and the transcriptome sequencing and population genomic investigations discovered the genome architecture, evolution, and domestication, which was valuable for understanding the genetic basis of important agronomic traits and breeding [1,5]. Besides, high-throughput proteomics analysis on spinach varieties of Sp73 and Sp75 revealed that heat perception, signal transduction, and reactive oxygen species (ROS) scavenging were crucial for the heat tolerance [3,4]. However, the finetuned heat-responsive molecular mechanism in spinach keeps unknown due to the lack of efficient genetic transformation system [6].
BSK is a critical family of receptor-like cytoplasmic kinase (RLCK) in the initial step, activating downstream phosphatase BSU1 for BR signal transduction [12]. Three Arabidopsis BSKs (i.e. AtBSK1, AtBSK2, and AtBSK3) have been identified as BR-responsive proteins [11]. The functions of some members among 12 Arabidopsis AtB-SKs and five rice OsBSKs have been well investigated, and they all have conserved kinase catalytic domain at N-terminus and tetratricopeptide repeats (TPRs) domain at C-terminus [11,[15][16][17]. Besides, myristoylation site at the N-terminus for plasma membrane (PM)-localization, critical serine (S) and lysine (K) sites (e.g., S 230 and K 104 in AtBSK1), as well as sumoylation and ubiquitination sites were also conserved in most AtBSKs [17].
During plant immunity response, BSK1 positively regulated pathogen-associated molecular pattern (PAMP)-trigged immunity (PTI) (i.e. edr-mediated resistance) by physically associating with the PAMP receptor FLAGELLIN SENSING2 (FLS2) in response PTI processes [18,30]. In addition, BSK8 was associated with FLS2 [31] and phosphorylated on flg22 treatment [32], although its molecular mechanism was still unclear. On the other hand, in the process of effector-triggered immunity (ETI) initiation, PM-localized BSK1 and BSK8 were identified as the components of Ribosomal protein S2 (RPS2) protein complex [31]. RPS2 is a well-studied resistance protein for the perception of pathogen. Therefore, BSKs played key roles in pathogen perception.
Interestingly, the dynamic spatiotemporal reorganization of BSK1 within PM was a crucial node for signalspecific activation of the balance between growth and immunity [33]. BSK1 multimerization and dissociation from the complexes of FLS2-BSK1 or BRI1-BSK1 were induced by the flg22 or exogenous BR treatment, respectively. Moreover, the flg22-triggered BSK1 translocated from membrane rafts to non-membrane raft regions for immunity response, whereas BR-induced BSK1 remained in membrane rafts for growth regulation [33].
In this study, seven members of the spinach BSK gene family were identified by screening the spinach wholegenome database [1,5]. The phylogenetic trees were constructed along with their homologous genes from sugar beet (Beta vulgaris), Arabidopsis, rice, maize, as well as common tobacco (Nicotiana tabacum) and woodland tobacco (Nicotiana sylvestris) for evaluating the evolution relationship and classification. The chromosomal distribution, gene structure, conserved function domains/ sites, and subcellular localization of SoBSKs were analyzed. Moreover, we examined the expression patterns of SoBSKs in different organs from heat-tolerant variety Sp75 and heat-sensitive variety Sp73, and upon exposure to temperature stresses and exogenous hormone treatments. Furthermore, diverse PTMs were found in several SoBSKs, implying the potential functions of SoBSKs. All these results lay a solid foundation for understanding the SoBSK-mediated molecular mechanisms in spinach development and stress response.

Phylogenetic relationship of BSKs from spinach and other plant species
To evaluate the evolution relationship of spinach BSKs with others, seven spinach BSKs, together with 65 BSKs from six representative model plants and/ or crops, were used to construct an un-rooted phylogenetic tree (Fig. 1). The protein sequences of seven BSKs from spinach, seven from sugar beet, 12 from Arabidopsis, 18 from common tobacco, 12 from woodland tobacco, five from rice, and 11 from maize were clustered in the phylogenetic tree ( Fig. 1 and Additional file 1). Among them, 12 Arabidopsis AtBSKs [11, 17-32, 40, 41], five rice OsBSKs [15,16], two woodland tobacco NsBSKs (i.e. NsBSK1 and NsBSK3) [42], a common tobacco NtBSK2 [42], and nine maize ZmBSKs [35] have been reported previously, and all the other sequences of BSKs were obtained by searching against the genome database using BLASTp.
Totally, 72 BSKs were grouped into seven classes (Class I to Class VII) (Fig. 1). Among them, seven SoBSKs distributed into four classes (Class I, Class II, Class V, and Class VII), while seven BSKs from monocotyledon rice and maize (in Class III and Class VI), as well as three BSKs from dicotyledon Arabidopsis (in Class IV) were grouped into the rest three classes, respectively (Fig. 1). Seven SoBSKs were grouped into unique subgroups with their homologous BSKs from sugar beets and Arabidopsis, but not tobacco species, while most BSKs from two tobacco species clustered together, except for NtBSK1 from common tobacco classed with AtBSK1 from Arabidopsis in a subgroup of Class I. The rest nine BSKs from monocotyledonous rice and maize distributed into two individual subgroups in Class I and Class II. Thus, the phylogenetic analysis indicated that these BSKs were highly conserved among monocotyledons and dicotyledons. Moreover, seven SoBSKs were closely homologous with BvBSKs from sugar beet, and also close to Arabidopsis BSKs rather than those from two tobacco species. This is consistent with the comparative genomics analysis and their evolutionary relationships [1].

Collinearity analysis of BSKs between spinach and other plants
The collinearity relationship was constructed between spinach and three plant species (i.e. Arabidopsis, sugar beet, and maize) (Fig. 2B). Collinearity analysis showed that SoBSKs had homologous genes in Arabidopsis, sugar beet, and maize, of which Arabidopsis had six homologous gene pairs located in chromosome 1, 4, and 5, followed by sugar beet (five gene pairs in chromosome 1, 7, and 8, as well as an unanchored scaffold chr5_nu.sca001), and maize (only one gene pair in chromosome 10) ( Fig. 2B and Additional file 2).

Gene structure and protein function domain analysis of SoBSKs
Phylogenetic analysis indicated that SoBSKs were grouped into three groups according to their amino acid sequences. SoBSK5, SoBSK6, and SoBSK4 were included in Group I, SoBSK1, SoBSK7, and SoBSK2 were classed into Group II, while SoBSK3 was a distinct Group III (Fig. 3A).
To predict the evolutionary feature and functional diversification, exon-intron organization of seven SoB-SKs was analyzed. SoBSK4 contained eleven introns, SoBSK2, SoBSK3, and SoBSK5 had nine introns, SoBSK1 and SoBSK7 had eight introns, while SoBSK6 had four introns (Fig. 3B). The diversity of various introns and exons implied the possible alternative splicing in SoBSKs was critical for spinach development and stress response, which were reported in Arabidopsis BSKs [17]. In addition, SoBSK4 and SoBSK6 only had 3'UTR, SoBSK5 only had 5'UTR, while the remaining four SoBSKs had both 5'UTR and 3'UTR (Fig. 3B).
The conserved motifs analysis suggested that thirteen conserved motifs were found in the six SoBSKs, except for SoBSK6 which only had seven motifs (Motif 1, 2, 4, 5, 8, 9, and 11) ( Fig. 3C and Additional file 3). Among 13 motifs, seven motifs (Motif 1, 3, 5, 6, 10, 11, and 12) were localized in the kinase domain, while three motifs (Motif 2, 4, and 9) were distributed in the TPR domain. Importantly, more than half amino acid sites (26 out of 50) in Motif 1 were highly conserved, among of which contained four conserved S sites (S22, S26, S36, and S43) (Fig. 3D). Besides, the 2nd serine in Motif 1 was also conserved in SoBSKs, except for SoBSK6 ( Fig. 3D and G). The Arabidopsis homologous site of the 2nd serine in Motif 1 (S 230 in AtBSK1 and S 210 in AtBSK3) had been reported to a phosphorylated site by AtBRI1 in the BR signaling pathway [11,16]. Moreover, the glycine (G)16, G28, and G37 in Motif 1 were also conserved in all SoBSKs ( Fig. 3D and G). The homologous sites in AtBSK3 of G16 and G28 (G 226 and G 238 in AtBSK3) can interfere other BSKs in BR signaling and protein stability of AtBSK3, respectively [21]. Motif 6 had 26 conserved amino acids out of 50 amino acids, including two lysines (K10 and K29 in Motif 6), and K29 was the key site for ATP binding and BSK kinase activity ( Fig. 3E and G) [21]. In addition, the 2nd glycine in Motif 13 was a highly conserved myristoylation site for membrane localization of BSKs ( Fig. 3F and G) [16,18].

Analyses of conserved function domains and modification sites in SoBSKs
A common feature of BSKs from Arabidopsis and rice is the presence of a N-terminal kinase domain and two or three C-terminal TPR domains, which can interact directly with each other for autoregulating its kinase activity [11,16]. In spinach, we also found the conserved N-terminal kinase domain and C-terminal TPR domains in seven SoBSKs (Fig. 3G). SoBSK2 and SoBSK3 contained two C-terminal TPR domains, but all the other SoBSKs had three C-terminal TPR domains (Fig. 3G).
We performed the prediction of some conserved amino acid sites for protein PTM. The sequence alignment with these reported functional sites in Arabidopsis [11,18,21,26,27,29,41] and rice [16], as well as the online tools GPS-SNO 1.0 [43] and UbiComb [44], were used for the predictions of phosphorylation, myristoylation, S-nitrosylation, and ubiquitination, respectively (Fig. 3G). Except for SoBSK6, all the other SoBSKs  Fig. 3G), which were the homologous sites with the conserved phosphorylated site by BRI1 and ATP-binding site for kinase activity determination in Arabidopsis, respectively [11,26]. Similarly, most SoBSKs, except for SoBSK6, had a glycine site for myristoylation modulating its PM localization, and more than one cystine for S-nitrosylation in response to nitric oxide signal [43] (Fig. 3G). In addition, SoBSK1 and SoBSK5 had a predicted ubiquitination site (K 100 in SoBSK1 and K 104 in SoBSK5) in the kinase domain (Fig. 3G), which were supposed to be a critical site for BSK degradation through ubiquitin-proteasome system. This indicated that these conserved PTM sites determined subcellular localization, redox regulation, and protein turnover of SoBSKs.

Localization of SoBSK1 and SoBSK6 proteins
The subcellular localization of SoBSKs was performed using tobacco leaves. SoBSK1 and SoBSK6 were fused respectively in frame to the 3'-terminus of the GFP reporter gene under the control of CaMV 35S promoter. The recombinant SoBSK1-GFP, SoBSK6-GFP, and GFP alone were transiently expressed in the epidermal cells of tobacco leaves. The 35S::GFP signals were distributed in the cytosol, nucleus, and PM in tobacco epidermal cells, while the signal from 35S::SoBSK1-GFP was concentrated in the PM (Fig. 5). This suggested that the SoBSK1-GFP recombinant protein localized on the cell membrane. Interestingly, unlike SoBSK1-GFP, SoBSK6-GFP recombinant protein localized not only in the cell membrane, but also in the cytoplasm and nucleus, because SoBSK6 was lack of the N-terminal myristoylation site for potential membrane localization [45]. This indicated that the truncated N-terminus without myristoylation site in SoBSK6 led to the missing of exclusive localization to cell periphery.

Organ-specific expression analysis of SoBSKs
To better understand organ-specific expression of seven SoBSK genes, total RNA from roots, stems, and three pairs of alternate leaves (i.e. the 1st, 2nd, and 3rd leaves) from heat-sensitive variety Sp73 and heat-tolerant variety Sp75 were prepared. The transcription level of each SoBSK gene was evaluated using reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) analysis ( Fig. 6 and Additional file 5). In heat-sensitive variety Sp73, SoBSK6 in stems, SoBSK3 in the 1st leaves, SoBSK4 in the 2nd leaves, and SoBSK2 in the 3rd leaves had the highest expression levels (Fig. 6). However, in heat-tolerant variety Sp75, SoBSK5 in stems, the 1st and 2nd leaves, as well as SoBSK4 in the 3rd leaves exhibited the highest expressions (Fig. 6). On the other hand, for each gene in variety Sp73, SoBSK1, SoBSK2, and SoBSK4 in the 3rd leaves, SoBSK3 in the 1st leaves, SoBSK5 and SoBSK7 in the roots, as well as SoBSK6 in the stems exhibited the highest expression (Fig. 6). While, in variety Sp75, it was SoBSK1 and SoBSK4 in the 3rd leaves, SoBSK2, SoBSK3, SoBSK5, and SoBSK6 in the 2nd leaves, as well as SoBSK7 in the roots that had the highest expression (Fig. 6). These suggested that, except of SoBSK7 in roots, the other SoBSKs mainly functioned in leaves rather than stems and roots in different varieties of spinach (Fig. 6).

ABA-and brassinolide (BL)-responses of SoBSKs in leaves
BSKs are critical components in BR signaling pathways [12]. We found multiple SoBSKs had ABRE cis-acting elements in their promoters for ABA signaling (Fig. 4). This implied that the cross-talk of BR and ABA signaling would happen in regulating plant growth, development, and stress response [46,47]. Therefore, we evaluated the expression profiles of seven SoBSKs in leaves under exogenous BL and ABA treatments using RT-qPCR analysis ( Fig. 7 and Additonal file 5).
For BL treatment, all the SoBSKs in variety Sp73 were induced more than 1.5-fold at 2 and 4 h. SoBSK1, SoBSK2, SoBSK3, SoBSK4, SoBSK5, and SoBSK7 reached their highest expression levels at 4 h, while SoBSK6 maintained a higher level with more than 2-fold during whole process (Fig. 7). Except of SoBSK1 and SoBSK3, the other SoBSKs in variety Sp73 were increased at 24 h (Fig. 7). However, in variety Sp75, SoBSK2, SoBSK3, and SoBSK5 were apparently induced at 2, 4, and 12 h, but reduced at 24 h (Fig. 7). Besides, SoBSK1 and SoBSK4 were increased, but SoBSK6 and SoBSK7 were decreased in variety Sp75 under most conditions (Fig. 7). These indicated that, although the seven SoBSKs were all involved in BL-response, most SoBSKs, except of SoBSK6 and SoBSK7, were BL-induced in both Sp73 and Sp75 at the early stages (2 and 4 h), and most SoBSKs exhibited significantly different even opposite responses in Sp73 and Sp75 under 24 h of BL treatment (Fig. 7). Interestingly, no SoBSKs were obviously ABA-induced in Sp73, and most of them were reduced in leaves under various exogenous ABA treatment conditions (Fig. 7). On the contrary, in Sp75, most SoBSKs in leaves were ABA-induced at 2 and 4 h, but ABA-reduced at 24 h (Fig. 7). All these suggested that heat-sensitive variety Sp73 and heat-tolerant variety Sp75 probably employed different BSK-mediated mechanisms in response to exogenous BR and ABA treatments.

Temperature stress-response of SoBSKs in leaves
Temperature extremes inhibit seed germination and reduce plant growth and reproduction [48]. We have predicted that 29 heat-responsive cis-acting elements and two cold-responsive cis-acting elements existed in SoBSKs promoters (Fig. 4). To evaluate the function of these SoBSKs in temperature response, the expression profiles of SoBSK genes in the heat-sensitive variety Sp73 and heat-tolerant variety Sp75 under heat and cold stresses were validated using RT-qPCR analysis. Most SoBSKs were significantly altered in both varieties under certain temperature stress condition when compared with the normal condition (0 h) ( Fig. 8 and Additional file 5). Importantly, the opposite temperatureresponsive expression patterns of most SoBSKs were observed in varieties of Sp73 and Sp75. Five SoBSKs, except of SoBSK1 and SoBSK6, were reduced in Sp73, but induced in Sp75 at 4 and 12 h of cold and heat stresses (Fig. 8). Under heat conditions, SoBSK2 and SoBSK4 were obviously decreased in Sp73, but SoBSK5 and SoBSK7 were increased at 12 and 24 h. However, five SoBSKs (i.e. SoBSK2, SoBSK3, SoBSK4, SoBSK5, and SoBSK7) were heat-induced in Sp75 under each time point, which was represented by the significantly heat-induced SoBSK2 (Fig. 8). The similar expression patterns were found under cold conditions. Five SoBSKs (i.e. SoBSK2, SoBSK3, SoBSK4, SoBSK5, and SoBSK7) were cold-increased in Sp75, but cold-decreased in Sp73, while two SoBSKs (i.e. SoBSK1 and SoBSK6) were slightly induced in Sp73, but reduced in Sp75 (Fig. 8).

Heat-responsive genes in BR-and ABA-signaling in leaves
The expression levels of six BR signaling-related genes and 16 ABA signaling-related genes were detected in leaves from variety Sp73 and variety Sp75 under heat treatments for 0, 2, 4, 12, and 24 h using RNA-sequencing assay ( Fig. 9 and Additional file 6). Two genes (BRL2 and BSK2) for BR signal perception were slightly heat-induced in variety Sp75 at 2 and 4 h, but significantly decreased in variety Sp73 at 12 and 24 h. However, the BKI1 for inhibition of BR binding with BRI1 was heat-reduced in Sp73 and Sp75 at 12 and 24 h (Fig. 9). Besides, three genes encoding transcription factors in the BR-mediated signaling pathway, including BZR1, BEH2, and BEH4, were induced in variety Sp75 under heat treatment (Fig. 9). This implied that BR signaling was probably employed in variety Sp75 for facilitating its heat tolerance.
The other 16 heat-altered genes were involved in ABA biosynthesis, transport, signal transduction, and transcriptional regulation (Fig. 9). Five genes for ABA biosynthesis, including two ZEPs, ABA4, NCED1, and NCED5, were reduced in variety Sp73, and four of them were also reduced in variety Sp75, except of NCED1 induced at 2 and 24 h (Fig. 9). Besides, ABCC2 for ABA transport from cytoplasm to vacuole was induced, but ABA efflux transporter ABCG25 and influx transporter ABCG22 for longdistance ABA transport were reduced in both Sp73 and  (Fig. 9). These indicated that the biosynthesis and transport of ABA were heat-disturbed in spinach, while some specific pathways probably were enhanced in heattolerant variety Sp75. Significantly, the expressions of four ABA receptor encoding genes (i.e. PYR1, PYL4, PYL5, and PYL9) were changed under heat treatments. Among them, PYL5 was significantly heat-induced in variety Sp73 and Sp75, and PYL4 was induced in Sp75 at 2 and 4 h (Fig. 9). Interestingly, PP2C24 and PP2C51, the negative regulation factor of ABA signaling, were obviously reduced in Sp75 under heat stress. Besides, the expressions of transcription factors ABI5 and AREB3 were altered, and AREB3 was increased in both Sp73 and Sp75 under heat treatments (Fig. 9). All these implied that variety Sp75 exhibited more enhanced ABA signaling to regulate heatresponsive process when compared with variety Sp73.

Heat-responsive phenotype of SoBSK1-overexpressing Arabidopsis plants
The SoBSK1 expression pattern was distinct with other SoBSKs in heat-tolerant variety Sp75 in response to heat treatment (Fig. 8). To investigate the function of SoBSK1 on heat tolerance, we constructed overexpressing SoBSK1 transgenic Arabidopsis plants under the control of the strong constitutive CaMV 35S promoter, and compared the survival rates of wild-type (WT), bsk134678 mutant, and SoBSK1-overexpressed seedlings under heat treatment (Fig. 10). Three-day-old WT, bsk134678 mutant, and SoBSK1-overexpressed seedlings grew under 22 °C for five days as control, or treated under 43 °C for 4 h, and following under 22 °C for five days as heat treatments ( Fig. 10A and B). There were no differences among WT, bsk134678 mutant, and SoBSK1-overexpressed seedlings under control condition, but they exhibited obvious different phenotypes under heat treatments (Fig. 10A). The bsk134678 mutant seedlings showed higher survival rate (92%), which was about 3.7-fold and 4.7-fold higher than WT and SoBSK1-overexpressed seedlings, respectively ( Fig. 10A and C). While WT and SoBSK1-overexpressed seedlings exhibited similar phenotype, and no significantly different survival rate was observed (Fig. 10C). These implied that SoBSK1 probably regulated plant heat tolerance as a negative factor and the members of BSK family had function redundance.

The SoBSKs had close homology with sugar beet BSKs
The BSKs belonged to the receptor-like cytoplasmic kinase superfamily RLCK-XII, which were firstly identified in A. thaliana [11]. Recently, the genome-wide identification of 143 BSKs from 17 representative plant species in different evolution positions has been reported [17]. Besides, the expression patterns of some members of BSKs were investigated in wild barley [36], Kentucky bluegrass [37], and P. tomentosa [38] in response to drought and cold, respectively. However, only a few of BSKs were cloned and characterized in plants, such as AtBSK1, AtBSK2, AtBSK3, and AtBSK5 in Arabidopsis [11, 18, 21-30, 33, 40], OsBSK1-2 and OsBSK3 in rice [15,16], NsBSK1 and NsBSK3 in woodland tobacco [42], NtBSK2 in common tobacco [42], and ZmBSK1 in maize [35]. The phylogenetic and functional analyses of BSKs from green vegetables, such as spinach, have not been reported so far.
In this study, seven SoBSK genes were identified in the genome and cloned from spinach variety Sp75. These SoBSKs, together with other 65 BSKs from Arabidopsis, sugar beet, common tobacco, woodland tobacco, rice, and maize, were grouped into seven classes in the phylogenetic tree (Fig. 1). Our results indicated that seven SoBSKs were closely homologous with BvBSKs from sugar beet, which was consistent with the results of whole-genome comparative analysis [1]. Sugar beet was another Caryophyllales species, which genome was relatively smaller (760 Mb) and closely related to spinach [1]. Moreover, the predicted number of proteincoding genes (25,495), the average length of the coding sequences (1157 bp), the number of average exons (5.3), and the number of transcription factors (1202) in spinach genome were all similar with those in sugar beet genome [1]. Therefore, BSK was a well-representative gene family revealing the close relationship between spinach and sugar beet.
In addition, our results indicated that the BSKs from dicotyledons (i.e. spinach, sugar beet, Arabidopsis, common tobacco, and woodland tobacco) and monocotyledons (i.e. rice and maize) were classed into separated subgroups in each class (Fig. 1), implying the lineagespecific evolution of BSK genes after the divergence of dicots and monocots. This was also found in the analysis of the genome-wide identification of 143 BSKs from 17 plant species, although spinach, common tobacco, woodland tobacco, and sugar beet were not included [17]. Interestingly, the expansion of BSK gene family attributed to the whole genome duplication (WGD) in some of the previously reported 17 plant species, such as two-fold expansion in Arabidopsis (12 BSKs), soybean (Glycine max) (13 BSKs), and Populus trichocarpa (14 BSKs), as well as three-fold expansion in Brassica rapa (21 BSKs) [17], but the WGD events were not observed in spinach (7 BSKs) [1]. Gene family members can be extended by duplication events under evolution processes [49]. It seems that the duplication events might have happened before species divergence in spinach.

SoBSKs had conserved TPR domain and kinase domain
Seven SoBSKs had conserved TPR domain at the C-terminus, including two TPRs in SoBSK2 and SoBSK3, and three TPRs in the other five SoBSKs (Fig. 3G). The conserved TPRs also existed in the BSKs from Arabidopsis [17] and rice [16]. TPR domain functioned to facilitate the specific interaction between partners acting as scaffolds for the assembly of multiprotein complexes [21,50]. The TPR in rice OsBSK3 was proved to an autoregulatory domain as a "phospho-switch" for modulating BSK kinase activity [16]. The TPR bound to the kinase domain of BSK3 for the prevention of BSK3 from binding to and activating BSU1 without BR signals, while the phosphorylated kinase domain of BSK3 by BR-activated BRI1 was free from the binding with the TPR domain, and then facilitated the binding affinity of BSKs for downstream phosphatase BSU1 to promote BR signaling pathway [16]. It has been found that TPR domain was critical for several BSK's functions in embryogenesis and defense responses [16,26,51]. In Arabidopsis, the missense mutation of the strictly conserved arginine (R) site R 443 (R443Q) in the TPR domain led to the loss-of-function of AtBSK1, conferring the defective defense responses [26]. Moreover, the TPR deletion of SSP/ BSK12 completely inactivated its function, resulting in the defective suspensor development upon Arabidopsis embryogenesis [51]. In rice, the TPR domain negatively regulated OsBSK3 activity in BR signaling [16]. On the contrary, the truncated AtBSK3 protein without TPR motifs (BSK3 TPR-Δ ) was less efficient to rescue the Arabidopsis root growth defect and BR resistance phenotype of bsk3-1 when compared with BSK3 protein, although it can fully complement the bsk3-1 mutant phenotypes. This indicated that TPR domain was not essential, but required for the full function of AtBSK3 in BR signaling [21]. Additionally, TPR deletion impaired the interactions of AtBSK3-AtBSK3 and AtBSK3-AtBSK1, implying its regulation to BSK homodimer and/ or heterodimer formation [21]. Interestingly, all the seven SoBSKs had the conserved TPR domain and R residue inside (Fig. 3G), which functions remained to be elucidated.
All SoBSKs contained conserved phosphorylation site of serine in the kinase domain, except of SoBSK6 (Fig. 3G). Their homologous serine sites in AtBSKs and OsBSKs were also conserved and critical for their kinase functions [11,16,26,41]. The S 230 in AtBSK1, S 210 in AtBSK3, S 209 and T 210 in AtBSK5, S 215 in OsBSK3, as well as the adjacent S, T, and Tyrosine (Y) residues in AtBSK6 and AtBSK8 have been reported to be phosphorylated by BRI1, RLK902, PEPR1, and ELONGATION FACTOR-TU RECEPTOR (EFR) and functioned in the BR signaling pathway upon plant immunity, respectively [11,16,18,29]. Phosphorylation events as a PTM can cause the critical changes in stability and activity of target proteins as well as protein-protein interactions [52,53]. Therefore, these conserved phosphorylation sites in SoBSKs would be pivotal for their functions in spinach development and stress response. Additionally, in the kinase domain, a lysine in six SoBSKs except of SoBSK6 were conserved, and two lysines (K 100 in SoBSK1 and K 104 in SoBSK5) were predicted to be ubiquitinated (Fig. 3G). The conserved lysine in six SoBSKs were homologous with K 104 in AtBSK1 [26], K 86 in AtBSK3 and AtBSK5 [18,21], as well as K 87 in AtBSK8 [54], which have been proved to the key sites of ATP binding for BSK kinase activity. However, the regulation role of this ubiquitination site in kinase domain for balancing the BSK degradation and its kinase activity needs to be investigated. Additionally, the conserved glycine sites in all SoBSKs (Fig. 3G) were homologous with G 238 and G 226 , which were found to interfere with the protein stability of AtBSK3 and other BSKs in BR signaling, respectively [21].

SoBSKs played important roles in spinach development and heat response
BSKs represent a critical kinase family that play partially redundant or overlapping roles in BR signaling and/ or other kinase signaling pathways during plant development and stress response [11,20]. In spinach, different SoBSK members displayed a constitutive and unique expression pattern in roots, stems, and leaves from variety Sp73 and variety Sp75, and most of them had higher expression in developing leaves (i.e. the 3rd and 2nd leaves) than that in the mature leaves (the 1st leaves) (Fig. 6), which implied SoBSKs were important for spinach growth and development. The similar expression patterns of BSKs were also found in Arabidopsis. Twelve AtBSKs were expressed in multiple tissues and organs (i.e. roots, flowers, rosette leaves, mature pollen, and seeds) during various developmental stages [17]. Phenotype analyses of various single, double, and multiple mutations of each AtBSK indicated that BSKs were partially redundant positive regulators of BR signaling in Arabidopsis [20]. Besides, the complex genetic interactions between BSKs (e.g., homodimers and/ or heterodimers) and their downstream proteins were supposed to the possible reasons for distinct functional characteristics of BSKs in diverse physiological and developmental processes [20].
In our results, most SoBSKs were BL-induced in leaves from both heat-sensitive variety Sp73 and heattolerant variety Sp75 (Fig. 7), which indicated that most SoBSKs were involved in the BR signaling pathway, and 2 to 4 h of BL treatments would be the critical time point for BR signal perception and original transduction in two spinach varieties. Importantly, several SoB-SKs (i.e. SoBSK2, SoBSK5, SoBSK6, and SoBSK7) were significantly ABA-induced in leaves from heat-tolerant variety Sp75, but ABA-reduced in heat-sensitive variety Sp73 under certain time points (Fig. 7). Moreover, SoBSK1 and SoBSK3 were highly heat-induced in variety Sp75 when compared with that in variety Sp73 (Fig. 7). This implied that heat-tolerant variety Sp75 potentially had stronger stress tolerance depending on ABA signaling pathway than heat-sensitive variety Sp73. Consistently, some AtBSKs were also significantly altered in response to various exogenous hormones (i.e., BL, ABA, JA, GA-3, Auxin, Zeatin, and 1-aminocyclopropane-1-carboxylic acid (ACC, ethylene precursor)) [17], implying that BSKs-mediated pathways had cross-talks with other hormone signaling pathways.
Importantly, our results indicated that the expression patterns of SoBSKs in leaves were altered under certain heat-and/ or cold-stress conditions, and most SoBSKs increased obviously in heat-tolerant variety Sp75 than those in heat-sensitive variety Sp73 (Fig. 8). Taken together with the ABA and drought responses of BSKs from Arabidopsis (i.e. AtBSK3, AtBSK5, and AtBSK8) and maize (ZmBSK1) [17,24,35], we supposed that BSKs were involved in the heat response via regulation of ABA-mediated stomatal closure and ROS homeostasis [24,55]. Thermotolerance assay of WT, bsk134678 mutant, and SoBSK1-overexpressed Arabidopsis seedlings suggested that SoBSKs participated in response to heat treatments redundantly, and SoBSK1 could be a negative regulator under heat conditions (Fig. 10). Besides, their homologous AtBSKs were also significantly altered under heat and cold conditions. Most AtBSKs were reduced under heat stress, but AtBSK1, AtBSK2, and AtBSK9 were induced in Arabidopsis under cold stress after 24 h [17]. Similarly, in Populus tomentosa, PtBSK, PtBRI1, and PtBIN2 were all increased under cold stress [38].
Additionally, the BSKs-mediated cross-talks of BR-signaling pathway and other pathways (e.g., ABA signaling, auxin signaling, ROS signaling, and MAPK cassette) were reported to function in diverse environment responses, such as salts [24,25,47,56,57], drought [17,35], low nitrogen [22], exogenous sucrose supply [41], as well as oxidative stress and wounding [17]. In this study, we evaluated the important gene expression in BR signaling and ABA signaling in spinach varieties Sp75 and Sp73 under heat stress using RNA-seq analysis. Our results indicated that heat-tolerant variety Sp75 was likely to improve heat resistance by promoting BRmediated downstream pathways through BR signaling transcription factors (i.e. BZR1, BEH2, and BEH4), and activating ABA signaling through regulating PYL4 and PP2Cs (Fig. 9). However, the key members and functions of BSKs in these fine-tuned modulation mechanisms, as well as the cross-talk of BR and ABA signaling still need to be investigated.

Identification and cloning of BSK genes in spinach
To identify the BSK family in spinach, the genome was downloaded from the SpinachBase (http:// www. spina chbase. org/). We used 12 AtBSK protein sequences as queries to search against the spinach genome database using BLASTp with an expected value (e-value) cutoff of 1E − 100 . Candidate SoBSKs were submitted to the NCBI web CD-search tool (https:// www. ncbi. nlm. nih. gov/ Struc ture/ bwrpsb/ bwrpsb. cgi) to verify their conserved kinase domain and TPR domain. To verify the accuracy of the predicted BSK sequences in spinach genome database, the coding sequences (CDSs) of BSKs were cloned with the SoBSKs primers (Additional file 7). The CDSs and protein sequences of SoBSKs were shown in Additional file 1.

Chromosomal distribution and collinearity analysis of SoBSK genes
The position information (e.g., chromosomal distribution, length, as well as the start and end positions) of SoBSK genes on the chromosome were obtained from SpinachBase, and visualized by MapGene2Chrom web v2 (http:// mg2c. iask. in/ mg2c_ v2.0/). The collinearity analysis of BSKs between the homologs in spinach and Arabidopsis, sugar beet, or maize were verified and visualized using One Stem MCScanX and Dual Systeny Plot for MCScanX in TBtools software, respectively.

Analyses of gene structure, function domain, conserved motif, and PTM
The exon-intron structure was analyzed based on the full-length genome sequences and the CDSs of SoBSKs by TBtools. Functional domains of SoBSKs were detected by the NCBI web CD-search tool. The conserved motifs of SoBSKs were determined by MEME (https:// meme-suite. org/ meme/ tools/ meme) using the protein sequences with the maximum motif number of 13, and were visualized by TBtools. The conserved phosphorylation, myristoylation, and reported conserved functional sites in SoBSKs were analyzed by sequence alignment with previous researches in Arabidopsis [11,18,21,26,27,29,41] and rice [16]. The S-nitrosylation and ubiquitination sites were predicted by GPS-SNO 1.0 [43] with default parameters and UbiComb (http:// nsclb io. jbnu. ac. kr/ tools/ UbiCo mb/) with a threshold value of 0.5 [44], respectively.

Identification of putative cis-regulatory elements in the promoters
The promoter sequences (2000 bp before the start codon) of all SoBSKs were extracted from the SpinachBase, and were analyzed by using the PlantCARE (http:// bioin forma tics. psb. ugent. be/ webto ols/ plant care/ html/) and visualized by TBtools.

Plant materials, RNA extraction, cDNA synthesis, and RT-qPCR
The spinach heat-sensitive variety Sp73 and heat-tolerant variety Sp75 were used for gene expression analysis [58]. The seeds were sown in a tray containing a perlitematrix (1:1) mixture and grown in a plant growth chamber. The growth conditions were set as 22 °C 10 h light/ 18 °C 14 h dark and 60% relative humidity [3]. The expression levels of SoBSK genes in various tissues including roots, stems, leaves (i.e. the 1st, 2nd, and 3rd leaves) were detected. Temperature stresses (4 °C for cold and 37 °C for heat) and exogenous hormone treatments (10 μM BL and 100 μM ABA) were applied for 0, 2, 4, 12, and 24 h with six-leaf stage of seedlings, respectively.
Total RNA was extracted from spinach leaves with TRIzol ™ LS Reagent (Invitrogen, USA) [59]. The RNA was reverse transcribed into cDNA using the Prime Script RT reagent kit. The RT-qPCR was performed using the SYBR Premix ExTaq II kit (TRAN, China) with SoARF as an internal control. Specific primer pairs were designed using Primer3 Web tool (http:// bioin fo. ut. ee/ prime r3/) (Additional file 7). RT-qPCR reactions were performed with three independent biological replicates. Besides, at least three technical replicates for some representative genes were performed in each set of RT-qPCR analyses (Additional file 5). Each gene was normalized to the SoARF internal control gene, and the relative gene expression was calculated according to the 2 -ΔΔCt method [60].

Differentially expressed genes (DEGs) analysis by RNA-sequencing
Total RNA was extracted from leaves of the spinach heat-sensitive variety Sp73 and heat-tolerant variety Sp75 after heat treatments at 0, 2, 4, 12, and 24 h using the mirVana miRNA Isolation Kit (Ambion). Three independent biological replicates were performed for RNAsequencing analysis (Additional file 6). RNA integrity was evaluated using the Agilent 2100 Bioanalyzer (Agilent Technologies, USA). The samples with RNA integrity number (RIN) ≥ 7 were subjected to enrich mRNA and construct cDNA libraries using TruSeq Stranded mRNA LTSample Prep Kit (Illumina, USA) according to the manufacturer's instructions. The libraries were sequenced on the HiSeq 2500 platform (Illumina, USA). The high-quality clean reads were obtained by removing adaptor sequences, empty reads low-quality bases (Q < 30) and used for transcriptome de novo assembly by mapping to spinach reference genome [1] using hisat2.
Fragments Per Kilobase of transcript per Million (FPKM) of each gene and read counts value of each transcript (protein_coding) were calculated using bowtie2 and eXpress. Differential expression analysis among the samples was performed using the DESeq (2012) R package. The genes with p value < 0.05 and Fold Change > 2 (or < 0.5) across the heat-stressed and control (0 h in heat-sensitive variety Sp73 or heat-tolerant variety Sp75) samples in at least two replicates were designated as DEGs in each variety.

Subcellular localization of SoBSK1 and SoBSK6
The open reading frames (ORFs) of SoBSK1 and SoBSK6 without stop codon were introduced into the plant expression vector pCAMBIA2300-GFP to produce SoBSK1-GFP and SoBSK6-GFP fusion proteins under the control of the CaMV 35S promoter. The resulting constructs (i.e. pCAMBIA2300-SoBSK1-GFP and pCAMBIA2300-SoBSK6-GFP) and the empty vector pCAMBIA2300-GFP were introduced into Agrobacterium tumefaciens strain EHA105. 35S::SoBSK1-GFP, 35S::SoBSK6-GFP, and 35S::GFP (the vector control) were introduced into six-week-old tobacco leaves by infiltration using needle-less syringes [61]. The instantaneously transformed tobacco leaves grew in dark for 24 h, following under normal conditions (25 °C 16 h light/ 20 °C 8 h dark) for 24 h. The GFP signals in transformed tobacco epidermal cells were visualized under an Olympus FV3000 confocal laser scanning microscope (Olympus, Japan). The GFP green fluorescent signals in 35S::SoBSK1-GFP and 35S::SoBSK6-GFP transformed tobacco epidermal cells, as well as their merged images with the chlorophyll fluorescence and bright field signals were used to determine the localization of SoBSK1 and SoBSK6 in the cell, respectively. The 35S::GFP was used as a control sample that showed the GFP fluorescence in the whole cell [62].

Thermotolerance analysis of transgenic Arabidopsis
The A. tumefaciens strain EHA105 cells containing pCAMBIA2300-SoBSK1-GFP plasmid were transformed into A. thaliana WT seedlings using the floral dip method [63] to obtain SoBSK1-overexpressed seedlings. The transformed seedlings were screened on 1/2 MS agar medium containing 50 μg/mL kanamycin for three generations. The SoBSK1 expression levels of several independently homozygous T3 lines were evaluated by RT-qPCR with gene-specific primers (Additional file 7), and the highest expressed line was selected for thermotolerance analysis. WT, bsk134678 mutant, and SoBSK1overexpressed A. thaliana seedlings were grown on 1/2 MS medium in a light incubator (22 °C 16 h light/ 20 °C 8 h dark, and 75% relative humidity) for eight days were control. The heat-treated seedlings were grown under control conditions for three days, then 43 °C for 4 h, and following under control conditions for five days. After treatments, the photographs were taken and the survival rates of seedlings from WT, bsk134678 mutant, and SoBSK1-overexpressed A. thaliana were calculated with three biologically independent replicates.